A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585309



Internal ID6625629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15330888..15332965hg38UCSC Ensembl
Innerchr1:15330937..15332917hg38UCSC Ensembl
Outerchr1:15330840..15333014hg38UCSC Ensembl
chr1:15657384..15659461hg19UCSC Ensembl
Innerchr1:15657433..15659413hg19UCSC Ensembl
Outerchr1:15657336..15659510hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863643
SamplesNA19703
Known GenesFHAD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585309
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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